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Retractor

EUDAMED

Class I (EU MDR)

Ref F16-266Model RETRACTOR

by Fairmount Industries Pvt Ltd

Identity

Device Name
RETRACTOR EUDAMED
Model / Reference
RETRACTOR EUDAMED
F16-266 EUDAMED

Identifiers

Primary DI / UDI-DI
+G742F162660K EUDAMED
Basic UDI-DI
++G742RETRACTORT8 EUDAMED
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Hand-held surgical retractor, reusable

Retractor by Fairmount Industries Pvt Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PK-MF-000044972
Authorised Representative
Maxcert Ltd XI-AR-000044423

Sources (1)

  • EUDAMED f3b55686-2ecc-45ee-8615-9e91533bb646 61 fields · synced Jun 18, 2026